From Form to Function: the Ways to Know a Neuron

References

• Bausenwein B., Fischbach K.-F. Activity labeling patterns in the medulla of Drosophila melanogaster caused by motion stimuli. Cell Tissue Res 1992; 270: 25–35
   PubMed Web of Science ®Google Scholar
• Bausenwein B., Dittrich A. P. M., Fischbach K.-F. The optic lobe of Drosophila melanogaster II. Sorting of retinotopic pathways in the medulla. Cell Tissue Res 1992; 267: 17–28
   PubMed Web of Science ®Google Scholar
• Bausenwein B., Buchner E., Heisenberg M. Identification of H1 visual interneuron in Drosophila by [3H]2-deoxyglucose uptake during stationary flight. Brain Res 1990; 12: 134–6
   Web of Science ®Google Scholar
• Betzig E., Patterson G. H., Sougrat R., Lindwasser O. W., Olenych S., Bonifacino J. S., et al. Imaging intracellular fluorescent proteins at nanometer resolution. Science 2006; 313: 1642–1645
   PubMed Web of Science ®Google Scholar
• Borst A., Haag J. The intrinsic electrophysiological characteristics of fly lobula plate tangential cells: I. Passive membrane properties. J Comput Neurosci 1996; 3: 313–336
   PubMed Web of Science ®Google Scholar
• Borst A., Haag J. Neural networks in the cockpit of the fly. J Comp Physiol A 2002; 188: 419–437
   PubMed Web of Science ®Google Scholar
• Brand A. H., Perrimon N. Targeted gene-expression as a means of altering cell fates and generating dominant phenotypes. Development 1993; 118: 401–415
   PubMed Web of Science ®Google Scholar
• Brunner A., Wolf R., Pflugfelder G. O., Poeck B., Heisenberg M. Mutations in the proximal region of the optomotor-blind locus of Drosophila melanogaster reveal a gradient of neuroanatomical and behavioral phenotypes. J Neurogenet 1992; 8: 43–55
   PubMed Web of Science ®Google Scholar
• Cajal, Ramon y, S. 1893. La rétine des vertébrás. La Cellule, 9, 119–257.
   Google Scholar
• Cajal, Ramon y, S. 1899. Textura del Sistema Nervioso del Hombre y de los Vertebrados. Madrid: Moya.
   Google Scholar
• Cajal, Ramon y, S. 1917. Contribución al conocimiento de la retina y centros ópticos de los cefalópodos. Trab Lab Invest Biol (Madrid), 15, 1–82.
   Google Scholar
• Cajal, Ramon y, S. 1937. Recollections of My Life (Recuerdos de Mi Vida). Horne Craigie, E., & Cano, J. (transl.). Cambridge, MassachusettsUSA: MIT Press.
   Google Scholar
• Cajal, Ramon y, S., & Sánchez, D. 1915. Contribución al conocimiento de los centros nerviosos de los insectos. Trab Lab Invest Biol (Madrid), 13, 1–164.
   Google Scholar
• Campos-Ortega J. A., Strausfeld N. J. Synaptic connections of intrinsic cells and basket arborizations in the external plexiform layer of the fly's eye. Brain Res 1973; 59: 119–136
   PubMed Web of Science ®Google Scholar
• Clements J., Lu Z., Gehring W. J., Meinertzhagen I. A., Callaerts P. Central projections of photoreceptor axons originating from ectopic eyes in Drosophila. Proc Natl Acad Sci USA 2008; 105: 8968–8973
   PubMed Web of Science ®Google Scholar
• Consoulas C., Levine R. B., Restifo L. L. The steroid hormone-regulated gene Broad Complex is required for dendritic growth of motoneurons during metamorphosis of Drosophila. J Comp Neurol 2005; 485: 321–337
   PubMed Web of Science ®Google Scholar
• Fahrenbach W. H. Anatomical circuitry of lateral inhibition in the eye of the horseshoe crab, Limulus polyphemus. Proc R Soc Lond B 1985; 225: 219–249
   PubMed Web of Science ®Google Scholar
• Feinberg E. H., Vanhoven M. K., Bendesky A., Wang G., Fetter R. D., Shen K., et al. GFP reconstitution across synaptic partners (GRASP) defines cell contacts and synapses in living nervous systems. Neuron 2008; 57: 353–363
   PubMed Web of Science ®Google Scholar
• Fischbach K.-F. Neural cell types surviving congenital sensory deprivation in the optic lobes of Drosophila melanogaster. Dev Biol 1983; 95: 1–18
   PubMed Web of Science ®Google Scholar
• Fischbach K.-F., Dittrich A. P. M. The optic lobe of Drosophila melanogaster. I. A Golgi analysis of wild-type structure. Cell Tissue Res 1989; 258: 441–475
   Web of Science ®Google Scholar
• Fischbach K.-F., Lyly-Hünerberg I. Genetic dissection of the anterior optic tract of Drosophila melanogaster. Cell Tissue Res 1983; 231: 551–563
   PubMed Web of Science ®Google Scholar
• Gao S., Takemura S-Y., Ting C-Y., Huang S., Lu Z., Luan H., et al. Neural substrate of spectral discrimination in Drosophila. Neuron 2008; 60: 328–342
   PubMed Web of Science ®Google Scholar
• Gengs C., Leung H. T., Skingsley D. R., Iovchev M. I., Yin Z., Semenov E. P., et al. The target of Drosophila photoreceptor synaptic transmission is a histamine-gated chloride channel encoded by ort (hclA). J Biol Chem 2002; 277: 42113–42120
   PubMed Web of Science ®Google Scholar
• Golgi C. Sulla sostanza grigia del cervello. Gazetta Med Ital (Lombardia) 1873; 6: 244–246
   Google Scholar
• Götz K. G. Optomotorische untersuchungen des visuellen systems einiger augenmutanten der fruchtfliege Drosophila. Kybernetik 1964; 2: 77–92
   PubMed Web of Science ®Google Scholar
• Graham R. C., Jr, Karnovsky M. J. The early stages of absorption of injected horseradish peroxidase in the proximal tubules of mouse kidney: ultrastructural cytochemistry by a new technique. J Histochem Cytochem 1966; 14: 291–302
   PubMed Web of Science ®Google Scholar
• Guerrero G., Isacoff E. Y. Genetically encoded optical sensors of neuronal activity and cellular function. Curr Opin Neurobiol 2001; 11: 601–607
   PubMed Web of Science ®Google Scholar
• Hanesch U., Fischbach K.-F., Heisenberg M. Neuronal architecture of the central complex in Drosophila melanogaster. Cell Tissue Res 1989; 257: 343–366
   Web of Science ®Google Scholar
• Hanström B. Vergleichende Anatomie des Nervensystems der wirbellosen Tiere. Julius Springer, Berlin 1928
   Google Scholar
• Hardie R. C. Is histamine a neurotransmitter in insect photoreceptors?. J Comp Physiol A 1987; 161: 201–213
   PubMed Web of Science ®Google Scholar
• Hausen K., Egelhaaf M. Neural mechanisms of visual course control in insects. Facets of Vision, D. G. Stavenga, R. C. Hardie. Springer, Berlin, Heidelberg, New York 1989; 391–424
   Google Scholar
• Hayworth K. J., Kasthuri N., Schalek R., Lichtman J. W. Automating the collection of ultrathin serial sections for large volume TEM reconstructions. Microsc Microanal 2006; 12(Supp 2)86–87
   Google Scholar
• Hecht S., Wald G. The influence of intensity on the visual functions of Drosophila. Proc Natl Acad Sci USA 1933; 19: 964–972
   PubMedGoogle Scholar
• Hecht S., Wald G. The visual acuity and intensity discrimination of Drosophila. J Gen Physiol 1934; 17: 517–547
   PubMedGoogle Scholar
• Heisenberg M., Borst A., Wagner S., Byers D. Drosophila mushroom body mutants are deficient in olfactory learning. J Neurogenet 1985; 2: 1–30
   PubMed Web of Science ®Google Scholar
• Heisenberg M., Buchner E. The role of retinula cell types in the visual behavior of Drosophila melanogaster. J Comp Physiol 1977; 117: 127–162
   Web of Science ®Google Scholar
• Heisenberg M., Wolf R. Vision in Drosophila. Springer-Verlag, Berlin, Heidelberg 1984
   Google Scholar
• Heisenberg M., Wonneberger R., Wolf R. optomotor-blindH31 —a Drosophila mutant of the lobula plate giant neurons. J Comp Physiol A 1978; 124: 287–296
   Web of Science ®Google Scholar
• Hotta Y., Benzer S. Genetic dissection of the Drosophila nervous system by means of mosaics. Proc Natl Acad Sci USA 1970; 67: 1156–1163
   PubMed Web of Science ®Google Scholar
• Hotta Y., Benzer S. Mapping of behaviour in Drosophila mosaics. Nature 1972; 240: 527–535
   PubMed Web of Science ®Google Scholar
• Huang B., Wang W., Bates M., Zhuang X. Three-dimensional super-resolution imaging by stochastic optical reconstruction microscopy. Science 2008; 319: 810–813
   PubMed Web of Science ®Google Scholar
• Ito K., Okada R., Tanaka N. K., Awasaki T. Cautionary observations on preparing and interpreting brain images using molecular biology-based staining techniques. Microsc Res Tech 2003; 62: 170–186
   PubMed Web of Science ®Google Scholar
• Jack J. J. B., Noble D., Tsien R. W. Electric Current Flow in Excitable Cells. Clarendon Press, Oxford 1975
   Google Scholar
• Joesch M., Plett J., Borst A., Reiff D. F. Response properties of motion-sensitive visual interneurons in the lobula plate of Drosophila melanogaster. Curr Biol 2008; 18: 368–374
   PubMed Web of Science ®Google Scholar
• Kalmus H. The optomotor responses of some eye mutants in Drosophila. J Genet 1943; 45: 206–213
   Google Scholar
• Kamikouchi A., Shimada T., Ito K. Comprehensive classification of the auditory sensory projections in the brain of the fruit fly Drosophila melanogaster. J Comp Neurol 2006; 499: 317–356
   PubMed Web of Science ®Google Scholar
• Katsov A. Y., Clandinin T. R. Motion processing streams in Drosophila are behaviorally specialized. Neuron 2008; 59: 322–335
   PubMed Web of Science ®Google Scholar
• Kitamoto T. Conditional modification of behavior in Drosophila by targeted expression of a temperature-sensitive shibire allele in defined neurons. J Neurobiol 2001; 47: 81–92
   PubMed Web of Science ®Google Scholar
• Klar, T. A., Engel, E., & Hell, S. W. 2001. Breaking Abbe's diffraction resolution limit in fluorescence microscopy with stimulated emission depletion beams of various shapes. Phys Rev E Stat Nonlin Soft Matter Phys, 64, 066613, 066611–066619.
   PubMed Web of Science ®Google Scholar
• Landgraf M., Bossing T., Technau G. M., Bate M. The origin, location, and projections of the embryonic abdominal motorneurons of Drosophila. J Neurosci 1997; 17: 9642–9655
   PubMed Web of Science ®Google Scholar
• Larsen C. W., Hirst E., Alexandre C., Vincent J. P. Segment boundary formation in Drosophila embryos. Development 2003; 130: 5625–5635
   PubMed Web of Science ®Google Scholar
• Lee T., Luo L. Mosaic analysis with a repressible cell marker for studies of gene function in neuronal morphogenesis. Neuron 1999; 22: 451–461
   PubMed Web of Science ®Google Scholar
• Liu G., Seiler H., Wen A., Zars T., Ito K., Wolf R., et al. Distinct memory traces for two visual features in the Drosophila brain. Nature 2006; 439: 551–556
   PubMed Web of Science ®Google Scholar
• Luan H., Peabody N. C., Vinson C. R., White B. H. Refined spatial manipulation of neuronal function by combinatorial restriction of transgene expression. Neuron 2006; 52: 425–436
   PubMed Web of Science ®Google Scholar
• Luo L., Callaway E. M., Svoboda K. Genetic dissection of neural circuits. Neuron 2008; 57: 634–660
   PubMed Web of Science ®Google Scholar
• Macagno E. R., LoPresti V., Levinthal C. Structure and development of neuronal connections in isogenic organisms: variations and similarities in the optic system of Daphnia magna. Proc Natl Acad Sci USA 1973; 70: 57–61
   PubMed Web of Science ®Google Scholar
• Marin E. C., Jefferis G. S., Komiyama T., Zhu H., Luo L. Representation of the glomerular olfactory map in the Drosophila brain. Cell 2002; 109: 243–255
   PubMed Web of Science ®Google Scholar
• Masland R. H. Neuronal cell types. Curr Biol 2004; 14: R497–R500
   PubMed Web of Science ®Google Scholar
• Meinertzhagen I. A., O'Neil S. D. Synaptic organization of columnar elements in the lamina of the wild type in Drosophila melanogaster. J Comp Neurol 1991; 305: 232–263
   PubMed Web of Science ®Google Scholar
• Meinertzhagen I. A., Sorra K. E. Synaptic organisation in the fly's optic lamina: few cells, many synapses, and divergent microcircuits. Progr Brain Res 2001; 131: 53–69
   PubMedGoogle Scholar
• Morante J., Desplan C. The color-vision circuit in the medulla of Drosophila. Curr Biol 2008; 18: 553–565
   PubMed Web of Science ®Google Scholar
• Nässel D. R. Horseradish peroxidase and other heme proteins as neuronal markers. Functional Neuroanatomy, N. J. Strausfeld. Springer-Verlag, Berlin, Heidelberg, New York 1983; 4–91
   Google Scholar
• Nässel D. R. Serotonin and serotonin-immunoreactive neurons in the nervous system of insects. Progr Neurobiol 1987; 30: 1–85
   Web of Science ®Google Scholar
• O'Keefe D. D., Thor S., Thomas J. B. Function and specificity of LIM domains in Drosophila nervous system and wing development. Development 1998; 125: 3915–3923
   PubMed Web of Science ®Google Scholar
• Otsuna H., Ito K. Systematic analysis of the visual projection neurons of Drosophila melanogaster. I. Lobula-specific pathways. J Comp Neurol 2006; 497: 928–958
   PubMed Web of Science ®Google Scholar
• Pfeiffer B. D., Jenett A., Hammonds A. S., Ngo T. T., Misra S., Murphy C., et al. Tools for neuroanatomy and neurogenetics in Drosophila. Proc Natl Acad Sci USA 2008; 105: 9715–9720
   PubMed Web of Science ®Google Scholar
• Rall W., Burke R. E., Holmes W. R., Jack J. J., Redman S. J., Segev I. Matching dendritic neuron models to experimental data. Physiol Rev 1992; 72(Suppl)S159–S186
   PubMed Web of Science ®Google Scholar
• Rister J., Pauls D., Schnell B., Ting C. Y., Lee C. H., Sinakevitch I., et al. Dissection of the peripheral motion channel in the visual system of Drosophila melanogaster. Neuron 2007; 56: 155–170
   PubMed Web of Science ®Google Scholar
• Sarthy P. V. Histamine: a neurotransmitter candidate for Drosophila photoreceptors. J Neurochem 1991; 57: 1757–1768
   PubMed Web of Science ®Google Scholar
• Schmid A., Hallermann S., Kittel R. J., Khorramshahi O., Frölich A. M., Quentin C., et al. Activity-dependent site-specific changes of glutamate receptor composition in vivo. Nat Neurosci 2008; 11: 659–656
   PubMed Web of Science ®Google Scholar
• Sjulson L., Miesenböck G. Rational optimization and imaging in vivo of a genetically encoded optical voltage reporter. J Neurosci 2008; 28: 5582–5593
   PubMed Web of Science ®Google Scholar
• Stocker R. F., Schorderet M. Cobalt filling of sensory projections from internal and external mouthparts in Drosophila. Cell Tissue Res 1981; 216: 513–523
   PubMed Web of Science ®Google Scholar
• Strausfeld N. J. Golgi studies on insects. Part II. The optic lobes of Diptera. Phil Trans Roy Soc Lond B 1970; 258: 135–223
   PubMed Web of Science ®Google Scholar
• Strausfeld N. J. The organization of the insect visual system (light microscopy). I. Projections and arrangements of neurons in the lamina ganglionaris of Diptera. Z Zellforsch 1971; 121: 377–441
   Google Scholar
• Strausfeld N. J. Atlas of an Insect Brain. Springer-Verlag, Berlin, Heidelberg 1976
   Google Scholar
• Strausfeld N. J. The Golgi method: its application to the insect nervous system and the phenomenon of stochastic impregnation. Neuroanatomical Techniques; Insect Nervous System, N. J. Strausfeld, T. A. Miller. Springer-Verlag, Berlin, Heidelberg, New York 1980; 131–203
   Google Scholar
• Strausfeld N. J., Douglass J., Campbell H., Higgins C. Parallel processing in the optic lobes of flies and the occurrence of motion computing circuits. Invertebrate Vision, E. Warrant, D.-E. Nilsson. Cambridge University Press, Cambridge 2006; 349–398
   Google Scholar
• Strausfeld N. J., Lee J-K. Neuronal basis for parallel visual processing in the fly. Vis Neurosci 1991; 7: 13–33
   PubMed Web of Science ®Google Scholar
• Strausfeld N. J., Seyan H. S., Wohlers D., Bacon J. P. Lucifer yellow histology. Functional Neuroanatomy, N. J. Strausfeld. Springer-Verlag, Berlin, Heidelberg, New York 1983; 132–155
   Google Scholar
• Strauss R., Heisenberg M. A higher control center of locomotor behavior in the Drosophila brain. J Neurosci 1993; 13: 1852–1861
   PubMed Web of Science ®Google Scholar
• Szentagothai J. What the “Reazione Nera” has given to us. Golgi Centennial Perspectives in Neurobiology, M. Santini. Raven Press, New York 1975; 1–12
   Google Scholar
• Takemura S., Lu Z., Meinertzhagen I. A. Synaptic circuits of the Drosophila optic lobe: the input terminals to the medulla. J Comp Neurol 2008; 509: 493–513
   PubMed Web of Science ®Google Scholar
• Tanaka N. K., Tanimoto H., Ito K. Neuronal assemblies of the Drosophila mushroom body. J Comp Neurol 2008; 508: 711–755
   PubMed Web of Science ®Google Scholar
• Tang S., Wolf R., Xu S., Heisenberg M. Visual pattern recognition in Drosophila is invariant for retinal position. Science 2004; 305: 1020–1022
   PubMed Web of Science ®Google Scholar
• Technau G. M. Fiber number in the mushroom bodies of adult Drosophila melanogaster depends on age, sex, and experience. J,. Neurogenet 1984; 1: 113–126
   PubMed Web of Science ®Google Scholar
• Wagh D. A., Rasse T. M., Asan E., Hofbauer A., Schwenkert I., Dürrbeck H., et al. Bruchpilot, a protein with homology to ELKS/CAST, is required for structural integrity and function of synaptic active zones in Drosophila. Neuron 2006; 49: 833–844
   PubMed Web of Science ®Google Scholar
• Wang J., Ma X., Yang J. S., Zheng X., Zugates C. T., Lee C. H., et al. Transmembrane/juxtamembrane domain-dependent Dscam distribution and function during mushroom body neuronal morphogenesis. Neuron 2004; 43: 663–72
   PubMed Web of Science ®Google Scholar
• White J. G., Southgate E., Thomson J. N., Brenner S. The structure of the nervous system of the nematode Caenorhabditis elegans. Phil Trans Roy Soc Lond Ser B 1986; 314: 1–340
   PubMed Web of Science ®Google Scholar
• Wong A. M., Wang J. W., Axel R. Spatial representation of the glomerular map in the Drosophila protocerebrum. Cell 2002; 109: 229–241
   PubMed Web of Science ®Google Scholar
• Zheng L., de Polavieja G. G., Wolfram V., Asyali M. H., Hardie R. C., Juusola M. Feedback network controls photoreceptor output at the layer of first visual synapses in Drosophila. J Gen Physiol 2006; 127: 495–510
   PubMed Web of Science ®Google Scholar